Cargando…
Long-Term Structural and Functional Assessment of Doyne Honeycomb Retinal Dystrophy following Nanosecond 2RT Laser Treatment: A Case Series
INTRODUCTION: Doyne honeycomb retinal dystrophy (DHRD), or autosomal dominant radial drusen, is a genetic disease caused by pathogenic variants of the epidermal growth factor (EGF)-containing fibulin-like extracellular matrix protein 1 EFEMP1 gene and is characterized by the formation of subretinal...
Autores principales: | Cusumano, Andrea, Falsini, Benedetto, D’Ambrosio, Michele, D’Apolito, Fabian, Sebastiani, Jacopo, Levialdi Ghiron, Jung Hee, Giardina, Emiliano, Cascella, Raffaella |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10666958/ https://www.ncbi.nlm.nih.gov/pubmed/38023612 http://dx.doi.org/10.1159/000534579 |
Ejemplares similares
-
Doyne honeycomb retinal dystrophy – functional improvement following subthreshold nanopulse laser treatment: a case report
por: Cusumano, Andrea, et al.
Publicado: (2019) -
Longitudinal Structure–Function Evaluation in a Patient with CDHR1-Associated Retinal Dystrophy: Progressive Visual Function Loss with Retinal Remodeling
por: Cusumano, Andrea, et al.
Publicado: (2023) -
A Splicing Variant in RDH8 Is Associated with Autosomal Recessive Stargardt Macular Dystrophy
por: Zampatti, Stefania, et al.
Publicado: (2023) -
Doyne honeycomb retinal dystrophy/malattia leventinese induced by EFEMP1 mutation in a Chinese family
por: Zhang, Kaiyan, et al.
Publicado: (2018) -
First reported case of Doyne honeycomb retinal dystrophy (Malattia Leventinese/autosomal dominant drusen) in Scandinavia
por: Sheyanth, Inger Norlyk, et al.
Publicado: (2021)